Joubert syndrome
A rare genetic syndrome characterized by the hypoplasia or absence of the cerebellar vermis. Signs and symptoms include rapid breathing (hyperpnea), sleep apnea, abnormal eye movements, mental retardation, and ataxia.
ICARE Institute of Medical Science and Research & B. C Roy Hospital
Associate Professor
SSKM&IPGMER
MD
Indraprastha Apollo Hospitals, New Delhi
Research Fellow
Government Medical College, Miraj
MBBS
Kerala Institute of Medical Sciences
Professor and Senior Consultant Neurology
Medical College Thiruvananthapuram
MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
MD and Consultant Radiologist Nivaran Scan Centre Latur, Nanded and Ambajogai
Dr Atul Deshmukh
Sir JJ Group Of Hospital, Mumbai
DMRD, DMRE
Atul Clinic
Consultant Physician
DAV Public School, Amritsar
Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )
NRS Medical College
MBBS Student
NRS Medical College
MBBS
Teerthankar Mahaveer Medical University
Consultant Neuruphysician
SMS Medical College ,Jaipur
DM neurology
Mahatma Gandhi Medical College and Research Institute
CRRI
Mahatma Gandhi Medical College and Research Institute
MBBS
Sri Padmavathi Medical College for Women
Medical Student
Svims
mbbs
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Diagnosis please. HSG.
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M.18yrs. Injury chest 2days.
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Mch.10yrs. Limping left 6 months.
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M.24yrs. A hard swelling at left high back 5 months. Chest-oblique view.
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F55yrs. Cough with sputum. Occassional haemoptysis 2 years. Breathlessness. 2 months
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